Multiple gastrointestinal stromal tumors in neurofibromatosis type 1: Report of a case

被引:0
|
作者
Kotaro Hirashima
Hiroshi Takamori
Masahiko Hirota
Hiroshi Tanaka
Atsushi Ichihara
Yasuo Sakamoto
Yoshiaki Ikuta
Ryu-Ichi Karashima
Masayuki Watanabe
Ken-Ichi Iyama
Hideo Baba
机构
[1] Kumamoto University,Department of Gastroenterological Surgery
[2] Kumamoto University,Department of Surgical Pathology, Graduate School of Medical Sciences
来源
Surgery Today | 2009年 / 39卷
关键词
Gastrointestinal stromal tumor; Neurofibromatosis type 1; c-kit; Platelet-derived growth factor receptor α; Mutation;
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学科分类号
摘要
This report presents a case of multiple gastrointestinal stromal tumors (GIST) with neurofibromatosis type 1 (NF1). A 68-year-old woman was admitted to the hospital because of a tumor close to the head of the pancreas. Imaging studies revealed submucosal tumors of the duodenum. The retroperitoneal tumor was diagnosed before surgery. Besides the main tumor in the duodenum, multiple small submucosal tumors were found in the duodenum and upper part of the jejunum during the operation. All of these tumors were resected. The histological diagnosis of all these tumors was GISTs. These tumors were immunohistochemically positive for KIT, but they demonstrated no mutation in c-kit exons 9, 11, 13, and 17, and platelet-derived growth factor receptor α exons 12 and 18. No recurrence occurred for a year after surgery.
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页码:979 / 983
页数:4
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